423-40-5Relevant academic research and scientific papers
PROCESS FOR PRODUCING PERFLUOROALKYLSULFONIC ACID SALT
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Page/Page column 9, (2011/11/07)
In this method for producing a perfluoroalkylsulfonic acid salt, there is provided a method for producing a perfluoroalkylsulfonic acid salt with a low fluorine content, which is a simple method to achieve a high yield, wherein a solution is formed by adding, to at least one compound selected from perfluoroalkylsulfonic acid salts represented by a general formula RfSO3?M (wherein Rf represents a perfluoroalkyl group of 1 to 4 carbon atoms, and M represents Li, Na or K), an organic solvent which is capable of dissolving the compound, and an adsorbent having a capacity to adsorb fluorine ions is added to the solution.
POTASSIUM PERFLUOROALKANESULFONATES AND PROCESS FOR PRODUCTION THEREOF
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Page/Page column 19-20, (2008/06/13)
A process for the production of potassium perfluoroalkane- sulfonates which comprises the electrolytic fluorination step of electrofluorinating an alkanesulfonyl halide in anhydrous hydrofluoric acid to obtain a gas containing a perfluoro- alkanesulfonyl fluoride as the main component. The process may further comprise the gas absorption step of reacting the gas with an aqueous solution of potassium hydroxide to form a solution containing a potassium perfluoroalkanesulfonate, the purification step of removing contaminant potassium fluoride, potassium hydroxide and potassium sulfate from the solution, and the concentration/recovery step of subjecting the purified aqueous solution to concentration and drying. In the electrolytic fluorination, the formation of by-products can be inhibited by keeping the proton concentration of the electrolytic solution within the range of 150 to 1500ppm.
Carbon-chain isomerization during the electrochemical fluorination in anhydrous hydrogen fluoride - A mechanistic study
Ignat'ev, Nikolai V.,Welz-Biermann, Urs,Heider, Udo,Kucheryna, Andriy,von Ahsen, Stefan,Habel, Wolfgang,Sartori, Peter,Willner, Helge
, p. 21 - 37 (2007/10/03)
The compounds i-C4H9SO2F, i-C3H7SO2F and cyclo-C3 H7C(O)F have been subjected to electrochemical fluorination in anhydrous hydrogen fluoride. The resulting products were fully analyzed by NMR spectroscopy. From the reaction balances, literature data and quantum chemical calculations, a new mechanism for carbon-chain isomerization during the electrochemical fluorination (ECF) is proposed. The key step in the formation of isomeric products is believed to be a ring closure reaction involving carbo-cationic or biradical intermediates.
Die elektrochemische fluorierung von alkansulfonamiden und alkandisulfonamiden
Satori,Juenger
, p. 71 - 75 (2007/10/03)
Alkane sulphonylamides and disulphonylamides are stable in anhydrous (HF)x and undergo quantitative fission of S-N bonds during electrochemical fluorination. Besides NF3, the corresponding perfluoroalkane sulphonyl fluorides and disulphonyl fluorides are formed.
